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. 2023 Feb 3;7(13):3117–3127. doi: 10.1182/bloodadvances.2022009411

Table 2.

Response rates in the efficacy-evaluable population

Response rates Efficacy-evaluable population (n = 147)
CRor CRh
 n (%) [95% CI] 51 (35) [27.0-43.0]
 Median time to CR/CRh, mo (range) 1.9 (0.9-5.6)
CR
 n (%) [95% CI] 47 (32) [24.5-40.2]
 Median time to CR, months (range) 2.8 (0.9-7.4)
Overall response
 N (%) [95% CI] 71 (48) [40.0-56.7]
 Median time to first overall response, mo (range) 1.9 (0.9-10.2)
Best overall response, n (%)
 CR 47 (32)
 CRh 4 (3)
 CRi 15 (10)
 PR 3 (2)
 MLFS 2 (1)
 SD 42 (29)
 Progressive disease 10 (7)
 Not evaluable/not done 6 (4) / 18 (12)

CRi, CR with incomplete blood count recovery; PR, partial remission; SD, stable disease (failure to achieve at least a PR but not meeting criteria for progressive disease. SD for a period of ≥8 weeks indicates clinical benefit).

Includes patients with CR, complete cytogenetic remission, and complete molecular remission.

Includes 3 patients considered to have clinical benefit by the treating physician and 2 patients considered to have resistant but stable disease.